JP2015511224A5 - - Google Patents
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- Publication number
- JP2015511224A5 JP2015511224A5 JP2014554840A JP2014554840A JP2015511224A5 JP 2015511224 A5 JP2015511224 A5 JP 2015511224A5 JP 2014554840 A JP2014554840 A JP 2014554840A JP 2014554840 A JP2014554840 A JP 2014554840A JP 2015511224 A5 JP2015511224 A5 JP 2015511224A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- isochromen
- amino
- pyrazin
- methylpiperazin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 122
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 26
- 125000003282 alkyl amino group Chemical group 0.000 claims 24
- 125000003545 alkoxy group Chemical group 0.000 claims 23
- 150000001875 compounds Chemical class 0.000 claims 14
- 125000000623 heterocyclic group Chemical group 0.000 claims 14
- 125000001072 heteroaryl group Chemical group 0.000 claims 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 9
- 208000002320 Spinal Muscular Atrophy Diseases 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 101710028394 SMN2 Proteins 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 3
- 102100007156 SMN1 Human genes 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- ZDZWYHMQADVMID-UHFFFAOYSA-N 3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-7-(4-propan-2-ylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(C(C)C)CCN1C1=CC=C(C=C(OC2=O)C=3N=C4C(C)=NC(C)=CN4C=3)C2=C1 ZDZWYHMQADVMID-UHFFFAOYSA-N 0.000 claims 2
- 108020004999 Messenger RNA Proteins 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000005241 heteroarylamino group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 claims 2
- 238000003780 insertion Methods 0.000 claims 2
- 229920002106 messenger RNA Polymers 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 239000011780 sodium chloride Substances 0.000 claims 2
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- -1 3- (6,8-dimethylimidazo [1,2-a] pyrazin-2-yl) -7- [4- (2-methoxypropyl) piperazin-1-yl] -1H-isochromen-1-one Chemical compound 0.000 claims 1
- SOUNGENGQBGPDJ-UHFFFAOYSA-N 3-(1,3-benzodioxol-5-yl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(C)CCN1C1=CC=C(C=C(OC2=O)C=3C=C4OCOC4=CC=3)C2=C1 SOUNGENGQBGPDJ-UHFFFAOYSA-N 0.000 claims 1
- JCVHRLIRCQUSLG-ZDUSSCGKSA-N 3-(1,3-benzodioxol-5-yl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1CN[C@@H](C)CN1C1=CC=C(C=C(OC2=O)C=3C=C4OCOC4=CC=3)C2=C1 JCVHRLIRCQUSLG-ZDUSSCGKSA-N 0.000 claims 1
- XGGJEBZNLNGURJ-UHFFFAOYSA-N 3-(1,3-benzodioxol-5-yl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=C2C(=O)OC(C=3C=C4OCOC4=CC=3)=CC2=CC=C1N1CCNCC1 XGGJEBZNLNGURJ-UHFFFAOYSA-N 0.000 claims 1
- RMMBPLGUTLDIOV-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-yl)-7-(1,4-diazepan-1-yl)isochromen-1-one Chemical compound C1=C2C(=O)OC(C=3SC4=CC=CC=C4N=3)=CC2=CC=C1N1CCCNCC1 RMMBPLGUTLDIOV-UHFFFAOYSA-N 0.000 claims 1
- WLGCJNFSWKPHKI-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-yl)-7-(4-methyl-1,4-diazepan-1-yl)isochromen-1-one Chemical compound C1CN(C)CCCN1C1=CC=C(C=C(OC2=O)C=3SC4=CC=CC=C4N=3)C2=C1 WLGCJNFSWKPHKI-UHFFFAOYSA-N 0.000 claims 1
- JNYYJCBZWIZAQL-ZDUSSCGKSA-N 3-(1,3-benzothiazol-2-yl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1CN[C@@H](C)CN1C1=CC=C(C=C(OC2=O)C=3SC4=CC=CC=C4N=3)C2=C1 JNYYJCBZWIZAQL-ZDUSSCGKSA-N 0.000 claims 1
- LFJUHEHZIGVYMZ-OKILXGFUSA-N 3-(1,3-benzothiazol-2-yl)-7-[(3S,5R)-3,5-dimethylpiperazin-1-yl]isochromen-1-one Chemical compound C1[C@@H](C)N[C@@H](C)CN1C1=CC=C(C=C(OC2=O)C=3SC4=CC=CC=C4N=3)C2=C1 LFJUHEHZIGVYMZ-OKILXGFUSA-N 0.000 claims 1
- DIDYFUQMYQIJOM-UHFFFAOYSA-N 3-(1,3-benzothiazol-2-yl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=C2C(=O)OC(C=3SC4=CC=CC=C4N=3)=CC2=CC=C1N1CCNCC1 DIDYFUQMYQIJOM-UHFFFAOYSA-N 0.000 claims 1
- VKOXUCHMDUPJHP-UHFFFAOYSA-N 3-(1,3-dimethylpyrrolo[1,2-a]pyrazin-7-yl)-7-(4-ethylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(CC)CCN1C1=CC=C(C=C(OC2=O)C3=CN4C=C(C)N=C(C)C4=C3)C2=C1 VKOXUCHMDUPJHP-UHFFFAOYSA-N 0.000 claims 1
- YMCDZHDCXLYIQP-UHFFFAOYSA-N 3-(1,3-dimethylpyrrolo[1,2-a]pyrazin-7-yl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(C)CCN1C1=CC=C(C=C(OC2=O)C3=CN4C=C(C)N=C(C)C4=C3)C2=C1 YMCDZHDCXLYIQP-UHFFFAOYSA-N 0.000 claims 1
- DFPPDGVHKSQRCP-UHFFFAOYSA-N 3-(1,3-dimethylpyrrolo[1,2-a]pyrazin-7-yl)-7-(4-propan-2-ylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(C(C)C)CCN1C1=CC=C(C=C(OC2=O)C3=CN4C=C(C)N=C(C)C4=C3)C2=C1 DFPPDGVHKSQRCP-UHFFFAOYSA-N 0.000 claims 1
- VWOLTIFBOYOVQN-UHFFFAOYSA-N 3-(1,3-dimethylpyrrolo[1,2-a]pyrazin-7-yl)-7-[4-(2-hydroxyethyl)piperazin-1-yl]isochromen-1-one Chemical compound C1=C2C(C)=NC(C)=CN2C=C1C(OC(=O)C1=C2)=CC1=CC=C2N1CCN(CCO)CC1 VWOLTIFBOYOVQN-UHFFFAOYSA-N 0.000 claims 1
- XAACNDLSCBBVDS-UHFFFAOYSA-N 3-(2,2-difluoro-1,3-benzodioxol-5-yl)-7-(4-methyl-1,4-diazepan-1-yl)isochromen-1-one Chemical compound C1CN(C)CCCN1C1=CC=C(C=C(OC2=O)C=3C=C4OC(F)(F)OC4=CC=3)C2=C1 XAACNDLSCBBVDS-UHFFFAOYSA-N 0.000 claims 1
- YOZIWSBPSOZHEJ-UHFFFAOYSA-N 3-(2,2-difluoro-1,3-benzodioxol-5-yl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=C2OC(F)(F)OC2=CC=C1C(OC(=O)C1=C2)=CC1=CC=C2N1CCNCC1 YOZIWSBPSOZHEJ-UHFFFAOYSA-N 0.000 claims 1
- YTYVDEJNLXRPOT-CQSZACIVSA-N 3-(2,3-dihydro-1,4-benzodioxin-6-yl)-7-[(3R)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1CN[C@H](C)CN1C1=CC=C(C=C(OC2=O)C=3C=C4OCCOC4=CC=3)C2=C1 YTYVDEJNLXRPOT-CQSZACIVSA-N 0.000 claims 1
- FFCATLDASLVELR-GASCZTMLSA-N 3-(2,3-dihydro-1,4-benzodioxin-6-yl)-7-[(3R,5S)-3,5-dimethylpiperazin-1-yl]isochromen-1-one Chemical compound C1[C@@H](C)N[C@@H](C)CN1C1=CC=C(C=C(OC2=O)C=3C=C4OCCOC4=CC=3)C2=C1 FFCATLDASLVELR-GASCZTMLSA-N 0.000 claims 1
- YTYVDEJNLXRPOT-AWEZNQCLSA-N 3-(2,3-dihydro-1,4-benzodioxin-6-yl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1CN[C@@H](C)CN1C1=CC=C(C=C(OC2=O)C=3C=C4OCCOC4=CC=3)C2=C1 YTYVDEJNLXRPOT-AWEZNQCLSA-N 0.000 claims 1
- DIHQRNHSZKEERZ-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzodioxin-6-yl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=C2C(=O)OC(C=3C=C4OCCOC4=CC=3)=CC2=CC=C1N1CCNCC1 DIHQRNHSZKEERZ-UHFFFAOYSA-N 0.000 claims 1
- FFDLILHNHGJPMY-AWEZNQCLSA-N 3-(2,4-dimethoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound COC1=CC(OC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 FFDLILHNHGJPMY-AWEZNQCLSA-N 0.000 claims 1
- XMTQKHGXZPDSNR-ZDUSSCGKSA-N 3-(2-fluoro-4-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound FC1=CC(OC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 XMTQKHGXZPDSNR-ZDUSSCGKSA-N 0.000 claims 1
- HZFQLHSZXSPVHS-UHFFFAOYSA-N 3-(2-methoxyphenyl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound COC1=CC=CC=C1C1=CC2=CC=C(N3CCN(C)CC3)C=C2C(=O)O1 HZFQLHSZXSPVHS-UHFFFAOYSA-N 0.000 claims 1
- LCBWCKJGIRYPMO-AWEZNQCLSA-N 3-(2-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound COC1=CC=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 LCBWCKJGIRYPMO-AWEZNQCLSA-N 0.000 claims 1
- AFKHSHXNKQEFCE-UHFFFAOYSA-N 3-(2-methyl-1,3-benzothiazol-5-yl)-7-piperazin-1-ylisochromen-1-one Chemical compound C=1C=C2SC(C)=NC2=CC=1C(OC(=O)C1=C2)=CC1=CC=C2N1CCNCC1 AFKHSHXNKQEFCE-UHFFFAOYSA-N 0.000 claims 1
- QKDCMLJYLGMSGK-UHFFFAOYSA-N 3-(2-methyl-1,3-benzothiazol-6-yl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(C)CCN1C1=CC=C(C=C(OC2=O)C=3C=C4SC(C)=NC4=CC=3)C2=C1 QKDCMLJYLGMSGK-UHFFFAOYSA-N 0.000 claims 1
- RUFXCZBKBSYKPD-UHFFFAOYSA-N 3-(2-methyl-1,3-benzothiazol-6-yl)-7-(4-propan-2-ylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(C(C)C)CCN1C1=CC=C(C=C(OC2=O)C=3C=C4SC(C)=NC4=CC=3)C2=C1 RUFXCZBKBSYKPD-UHFFFAOYSA-N 0.000 claims 1
- HVDQRLLJJQHVCY-UHFFFAOYSA-N 3-(2-methyl-1,3-benzothiazol-6-yl)-7-[4-(oxetan-3-yl)piperazin-1-yl]isochromen-1-one Chemical compound C1=C2SC(C)=NC2=CC=C1C(OC(=O)C1=C2)=CC1=CC=C2N(CC1)CCN1C1COC1 HVDQRLLJJQHVCY-UHFFFAOYSA-N 0.000 claims 1
- RMSZLJVANBXOAW-UHFFFAOYSA-N 3-(2-methyl-1,3-benzothiazol-6-yl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=C2SC(C)=NC2=CC=C1C(OC(=O)C1=C2)=CC1=CC=C2N1CCNCC1 RMSZLJVANBXOAW-UHFFFAOYSA-N 0.000 claims 1
- JVUVATSKMZPTBI-UHFFFAOYSA-N 3-(2-methylindazol-5-yl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound C1CN(C)CCN1C1=CC=C(C=C(OC2=O)C3=CC4=CN(C)N=C4C=C3)C2=C1 JVUVATSKMZPTBI-UHFFFAOYSA-N 0.000 claims 1
- VJHJOFDYLVZNCO-UHFFFAOYSA-N 3-(2-methylindazol-5-yl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=CC2=NN(C)C=C2C=C1C(OC(=O)C1=C2)=CC1=CC=C2N1CCNCC1 VJHJOFDYLVZNCO-UHFFFAOYSA-N 0.000 claims 1
- AOYUTKODKWDUOP-LBPRGKRZSA-N 3-(3,4-dihydroxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1CN[C@@H](C)CN1C1=CC=C(C=C(OC2=O)C=3C=C(O)C(O)=CC=3)C2=C1 AOYUTKODKWDUOP-LBPRGKRZSA-N 0.000 claims 1
- DUHICLNDLDBYTH-UHFFFAOYSA-N 3-(3,4-dimethoxyphenyl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC2=CC=C(N3CCN(C)CC3)C=C2C(=O)O1 DUHICLNDLDBYTH-UHFFFAOYSA-N 0.000 claims 1
- NJYZJCOUGJGYDI-GASCZTMLSA-N 3-(3,4-dimethoxyphenyl)-7-[(3R,5S)-3,5-dimethylpiperazin-1-yl]isochromen-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC2=CC=C(N3C[C@@H](C)N[C@@H](C)C3)C=C2C(=O)O1 NJYZJCOUGJGYDI-GASCZTMLSA-N 0.000 claims 1
- FBJDRSNXLDHKBO-HNNXBMFYSA-N 3-(3,4-dimethoxyphenyl)-7-[(3S)-3,4-dimethylpiperazin-1-yl]isochromen-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)N(C)CC3)C=C2C(=O)O1 FBJDRSNXLDHKBO-HNNXBMFYSA-N 0.000 claims 1
- FFVOWQLMMLMKRX-AWEZNQCLSA-N 3-(3,4-dimethoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 FFVOWQLMMLMKRX-AWEZNQCLSA-N 0.000 claims 1
- YLMGJLMUAAUMNC-UHFFFAOYSA-N 3-(3,4-dimethoxyphenyl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC2=CC=C(N3CCNCC3)C=C2C(=O)O1 YLMGJLMUAAUMNC-UHFFFAOYSA-N 0.000 claims 1
- OSEFOZOIABHORM-LBPRGKRZSA-N 3-(3,5-difluoro-4-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1=C(F)C(OC)=C(F)C=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 OSEFOZOIABHORM-LBPRGKRZSA-N 0.000 claims 1
- USOVNYDOTAWWKX-UHFFFAOYSA-N 3-(3,5-difluorophenyl)-7-piperazin-1-ylisochromen-1-one Chemical compound FC1=CC(F)=CC(C=2OC(=O)C3=CC(=CC=C3C=2)N2CCNCC2)=C1 USOVNYDOTAWWKX-UHFFFAOYSA-N 0.000 claims 1
- JHAIIMZPZCLZKV-ZDUSSCGKSA-N 3-(3-chloro-4-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1=C(Cl)C(OC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 JHAIIMZPZCLZKV-ZDUSSCGKSA-N 0.000 claims 1
- AHRDCSGRRJKJEX-ZDUSSCGKSA-N 3-(3-fluoro-4-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1=C(F)C(OC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 AHRDCSGRRJKJEX-ZDUSSCGKSA-N 0.000 claims 1
- RFTDWCCIVAWAQL-ZDUSSCGKSA-N 3-(3-hydroxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1CN[C@@H](C)CN1C1=CC=C(C=C(OC2=O)C=3C=C(O)C=CC=3)C2=C1 RFTDWCCIVAWAQL-ZDUSSCGKSA-N 0.000 claims 1
- OVBYKFYQWNTJDM-UHFFFAOYSA-N 3-(3-methoxyphenyl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound COC1=CC=CC(C=2OC(=O)C3=CC(=CC=C3C=2)N2CCN(C)CC2)=C1 OVBYKFYQWNTJDM-UHFFFAOYSA-N 0.000 claims 1
- IWIIBNHQUADCAW-UHFFFAOYSA-N 3-(3-methoxyphenyl)-7-piperazin-1-ylisochromen-1-one Chemical compound COC1=CC=CC(C=2OC(=O)C3=CC(=CC=C3C=2)N2CCNCC2)=C1 IWIIBNHQUADCAW-UHFFFAOYSA-N 0.000 claims 1
- BCWJBGUYUSAWDB-HNNXBMFYSA-N 3-(4-ethoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1=CC(OCC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 BCWJBGUYUSAWDB-HNNXBMFYSA-N 0.000 claims 1
- QCZRHNHWJXCHCP-UHFFFAOYSA-N 3-(4-ethoxyphenyl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=CC(OCC)=CC=C1C1=CC2=CC=C(N3CCNCC3)C=C2C(=O)O1 QCZRHNHWJXCHCP-UHFFFAOYSA-N 0.000 claims 1
- DZXVPQVQYHFRHK-ZDUSSCGKSA-N 3-(4-fluoro-3-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1=C(F)C(OC)=CC(C=2OC(=O)C3=CC(=CC=C3C=2)N2C[C@H](C)NCC2)=C1 DZXVPQVQYHFRHK-ZDUSSCGKSA-N 0.000 claims 1
- SJQCCYLDNFCWHV-UHFFFAOYSA-N 3-(4-methoxyphenyl)-7-(4-methylpiperazin-1-yl)isochromen-1-one Chemical compound C1=CC(OC)=CC=C1C1=CC2=CC=C(N3CCN(C)CC3)C=C2C(=O)O1 SJQCCYLDNFCWHV-UHFFFAOYSA-N 0.000 claims 1
- PRRLCIVMXKUMIM-AWEZNQCLSA-N 3-(4-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound C1=CC(OC)=CC=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 PRRLCIVMXKUMIM-AWEZNQCLSA-N 0.000 claims 1
- AQQCUSSDYYCHML-UHFFFAOYSA-N 3-(4-methoxyphenyl)-7-piperazin-1-ylisochromen-1-one Chemical compound C1=CC(OC)=CC=C1C1=CC2=CC=C(N3CCNCC3)C=C2C(=O)O1 AQQCUSSDYYCHML-UHFFFAOYSA-N 0.000 claims 1
- PNSHLQYQODCZBP-ZDUSSCGKSA-N 3-(5-fluoro-2-methoxyphenyl)-7-[(3S)-3-methylpiperazin-1-yl]isochromen-1-one Chemical compound COC1=CC=C(F)C=C1C1=CC2=CC=C(N3C[C@H](C)NCC3)C=C2C(=O)O1 PNSHLQYQODCZBP-ZDUSSCGKSA-N 0.000 claims 1
- XXQSIQIKTMDLDE-UHFFFAOYSA-N 3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-7-(1,2,3,6-tetrahydropyridin-4-yl)isochromen-1-one Chemical compound N1=C2C(C)=NC(C)=CN2C=C1C(OC(=O)C1=C2)=CC1=CC=C2C1=CCNCC1 XXQSIQIKTMDLDE-UHFFFAOYSA-N 0.000 claims 1
- GUMCGNFWXMALGM-UHFFFAOYSA-N 3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-7-(1-ethyl-3,6-dihydro-2H-pyridin-4-yl)isochromen-1-one Chemical compound C1N(CC)CCC(C=2C=C3C(=O)OC(=CC3=CC=2)C=2N=C3C(C)=NC(C)=CN3C=2)=C1 GUMCGNFWXMALGM-UHFFFAOYSA-N 0.000 claims 1
- IFFFIGBSTGOFBF-UHFFFAOYSA-N 3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-7-(1-ethylpiperidin-4-yl)isochromen-1-one Chemical compound C1CN(CC)CCC1C1=CC=C(C=C(OC2=O)C=3N=C4C(C)=NC(C)=CN4C=3)C2=C1 IFFFIGBSTGOFBF-UHFFFAOYSA-N 0.000 claims 1
- ZVSGJGATQDYOQK-UHFFFAOYSA-N 3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-7-(1-methylpiperidin-4-yl)isochromen-1-one Chemical compound C1CN(C)CCC1C1=CC=C(C=C(OC2=O)C=3N=C4C(C)=NC(C)=CN4C=3)C2=C1 ZVSGJGATQDYOQK-UHFFFAOYSA-N 0.000 claims 1
- CVAXFFBONNMMNT-UHFFFAOYSA-N 3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-7-(1-propan-2-yl-3,6-dihydro-2H-pyridin-4-yl)isochromen-1-one Chemical compound C1N(C(C)C)CCC(C=2C=C3C(=O)OC(=CC3=CC=2)C=2N=C3C(C)=NC(C)=CN3C=2)=C1 CVAXFFBONNMMNT-UHFFFAOYSA-N 0.000 claims 1
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| EA029984B1 (ru) | 2011-12-30 | 2018-06-29 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Соединения для лечения спинальной мышечной атрофии |
| CA2862084C (en) * | 2012-01-26 | 2021-05-11 | Ptc Therapeutics, Inc. | 1h-isochromen-1-one derivatives and compositions thereof for treating spinal muscular atrophy |
| EA037123B1 (ru) | 2012-02-10 | 2021-02-09 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Соединения для лечения спинальной мышечной атрофии |
| JP6092264B2 (ja) | 2012-03-01 | 2017-03-08 | ピーティーシー セラピューティクス， インコーポレイテッド | 脊髄性筋委縮症を処置するための化合物 |
| BR112014023483B1 (pt) | 2012-03-23 | 2022-05-10 | Ptc Therapeutics, Inc | Composto e seu uso, composição farmacêutica e seu uso |
| WO2014102778A2 (en) * | 2012-12-24 | 2014-07-03 | Ramot At Tel-Aviv University Ltd. | Agents for treating genetic diseases resulting from nonsense mutations, and methods for identifying the same |
| WO2015024876A2 (en) | 2013-08-19 | 2015-02-26 | F. Hoffmann-La Roche Ag | Screening method |
| WO2015105657A1 (en) | 2013-12-19 | 2015-07-16 | Ptc Therapeutics, Inc. | Methods for modulating the amount of rna transcripts |
| WO2015095446A1 (en) * | 2013-12-19 | 2015-06-25 | Ptc Therapeutics, Inc. | Methods for modulating the amount of rna transcripts |
| US10882868B2 (en) | 2014-05-15 | 2021-01-05 | Hoffmann-La Roche Inc. | Compounds for treating spinal muscular atrophy |
| EP4249472A3 (en) | 2015-05-30 | 2023-12-13 | PTC Therapeutics, Inc. | Methods for modulating rna splicing |
| PL3373972T3 (pl) * | 2015-11-12 | 2024-06-17 | F. Hoffmann-La Roche Ag | Kompozycje do leczenia rdzeniowego zaniku mięśni |
| EP3377073A4 (en) | 2015-11-16 | 2019-06-26 | Ohio State Innovation Foundation | METHOD AND COMPOSITIONS FOR TREATING DISORDERS AND DISEASES WITH THE SURVIVAL MOTOR NEURON (SMN) PROTEIN |
| CN108137579B (zh) | 2015-12-10 | 2022-01-07 | 豪夫迈·罗氏有限公司 | 桥连哌啶衍生物 |
| AU2016366694C1 (en) | 2015-12-10 | 2021-03-25 | Ptc Therapeutics, Inc. | Methods for treating huntington's disease |
| JP6738044B2 (ja) * | 2016-07-22 | 2020-08-12 | Jnc株式会社 | ベンゾピラン骨格を有する液晶性化合物、液晶組成物、および液晶表示素子 |
| AU2017363369A1 (en) | 2016-11-28 | 2019-05-30 | Ptc Therapeutics, Inc | Methods for modulating RNA splicing |
| KR20200033249A (ko) | 2017-06-05 | 2020-03-27 | 피티씨 테라퓨틱스, 인크. | 헌팅턴병 치료 화합물 |
| US11608501B2 (en) | 2017-06-14 | 2023-03-21 | Ptc Therapeutics, Inc. | Methods for modifying RNA splicing |
| MX2019015578A (es) | 2017-06-28 | 2020-07-28 | Ptc Therapeutics Inc | Metodos para tratar la enfermedad de huntington. |
| MX2019015580A (es) | 2017-06-28 | 2020-07-28 | Ptc Therapeutics Inc | Metodos para tratar la enfermedad de huntington. |
| MX2020001425A (es) | 2017-08-04 | 2020-08-06 | Skyhawk Therapeutics Inc | Metodos y composiciones para modular el empalme. |
| JP7399870B2 (ja) | 2018-03-27 | 2023-12-18 | ピーティーシー セラピューティクス， インコーポレイテッド | ハンチントン病を処置するための化合物 |
| BR112020026637A2 (pt) * | 2018-06-27 | 2021-03-30 | Reborna Biosciences, Inc. | Agente profilático ou terapêutico para atrofia muscular espinhal |
| DK3814357T3 (da) | 2018-06-27 | 2024-07-22 | Ptc Therapeutics Inc | Heterocykliske og heteroarylforbindelser til behandling af huntingtons sygdom |
| EP3814360A1 (en) | 2018-06-27 | 2021-05-05 | PTC Therapeutics, Inc. | Heteroaryl compounds for treating huntington's disease |
| EP3920915A4 (en) | 2019-02-05 | 2022-10-05 | Skyhawk Therapeutics, Inc. | METHODS AND COMPOSITIONS FOR MODULATING SPLICE |
| KR20210135507A (ko) | 2019-02-06 | 2021-11-15 | 스카이호크 테라퓨틱스, 인코포레이티드 | 스플라이싱을 조절하는 방법 및 조성물 |
| US11129829B2 (en) | 2019-06-17 | 2021-09-28 | Skyhawk Therapeutics, Inc. | Methods for modulating splicing |
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| JPS5854142B2 (ja) * | 1975-04-16 | 1983-12-02 | 株式会社興人 | イソカルボスチリル誘導体の製造方法 |
| US5089633A (en) | 1987-04-28 | 1992-02-18 | Georgia Tech Research Corporation | Substituted isocoumarins |
| US6180625B1 (en) * | 1998-03-24 | 2001-01-30 | Novo Nordisk A/S | Heterocyclic compounds regulating clotting |
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| GB0205281D0 (en) * | 2002-03-06 | 2002-04-17 | Novartis Ag | Organic compounds |
| WO2003104216A1 (en) * | 2002-06-10 | 2003-12-18 | Acadia Pharmaceuticals Inc. | Urotensin ii receptor modulators |
| US7553852B2 (en) * | 2002-06-28 | 2009-06-30 | Vertex Pharmaceuticals Incorporated | Caspase inhibitors and uses thereof |
| JP2004168707A (ja) * | 2002-11-20 | 2004-06-17 | Bayer Cropscience Ag | イソチアゾリルベンゾオキサジン誘導体および病害防除剤 |
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| JP2008528496A (ja) | 2005-01-21 | 2008-07-31 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | エストロゲン受容体のモジュレーターとして有用な新規な複素環式ベンゾ［ｃ］クロメン誘導体 |
| KR100781704B1 (ko) | 2005-04-20 | 2007-12-03 | 에스케이케미칼주식회사 | 피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물 |
| AR059339A1 (es) | 2006-02-09 | 2008-03-26 | Chugai Pharmaceutical Co Ltd | Derivados de la cumarina para trastornos proliferativos de celulas, composicion farmaceutica y agente terapeutico que los contiene |
| WO2008013997A2 (en) | 2006-07-27 | 2008-01-31 | The Trustees Of Columbia University In The City Of New York | Fluorescent substrates for monoamine transporters as optical false neurotransmitters |
| KR20080091949A (ko) | 2007-04-10 | 2008-10-15 | 에스케이케미칼주식회사 | 락톤형 피리딘 화합물을 포함하는 허혈성 질환의 예방 및치료용 약학조성물 |
| JP5276878B2 (ja) * | 2007-09-27 | 2013-08-28 | 富士フイルム株式会社 | ベンゾオキサジノン系化合物の製造方法 |
| US8633019B2 (en) * | 2008-05-27 | 2014-01-21 | Ptc Therapeutics, Inc. | Methods for treating spinal muscular atrophy |
| US8986935B2 (en) | 2008-08-13 | 2015-03-24 | Ptc Therapeutics, Inc. | Methods for treating spinal muscular atrophy |
| EA029984B1 (ru) | 2011-12-30 | 2018-06-29 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Соединения для лечения спинальной мышечной атрофии |
| CA2862084C (en) * | 2012-01-26 | 2021-05-11 | Ptc Therapeutics, Inc. | 1h-isochromen-1-one derivatives and compositions thereof for treating spinal muscular atrophy |
| EA037123B1 (ru) | 2012-02-10 | 2021-02-09 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Соединения для лечения спинальной мышечной атрофии |
| JP6092264B2 (ja) | 2012-03-01 | 2017-03-08 | ピーティーシー セラピューティクス， インコーポレイテッド | 脊髄性筋委縮症を処置するための化合物 |
| BR112014023483B1 (pt) | 2012-03-23 | 2022-05-10 | Ptc Therapeutics, Inc | Composto e seu uso, composição farmacêutica e seu uso |
-
2013
- 2013-01-25 CA CA2862084A patent/CA2862084C/en active Active
- 2013-01-25 EP EP13740919.9A patent/EP2809322B9/en active Active
- 2013-01-25 EA EA201491412A patent/EA028344B1/ru not_active IP Right Cessation
- 2013-01-25 KR KR1020147023617A patent/KR102064624B1/ko active IP Right Grant
- 2013-01-25 CN CN201380016999.2A patent/CN104203239B/zh active Active
- 2013-01-25 US US14/373,937 patent/US9399649B2/en active Active
- 2013-01-25 WO PCT/US2013/023067 patent/WO2013112788A1/en active Application Filing
- 2013-01-25 ES ES13740919T patent/ES2733644T3/es active Active
- 2013-01-25 BR BR112014018027-0A patent/BR112014018027B1/pt active IP Right Grant
- 2013-01-25 JP JP2014554840A patent/JP6193888B2/ja active Active
- 2013-01-25 MX MX2014008875A patent/MX357834B/es active IP Right Grant
- 2013-01-25 PL PL13740919T patent/PL2809322T3/pl unknown
-
2015
- 2015-03-16 HK HK15102661.7A patent/HK1202069A1/xx unknown
-
2017
- 2017-04-20 JP JP2017083760A patent/JP2017171667A/ja active Pending
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